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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147436insertion1nstd232human GRCh37.p13 chr21: 44,261,545-44,261,545 , GRCh38.p12 chr21: 42,841,435-42,841,435 WDR4
    nsv7096096copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr21: 43,160,998-47,754,702 , GRCh38.p12 chr21: 41,740,838-46,334,788 TSPEAR, LINC01424, 158 more genes
    nsv7095922copy number variation1nstd102humanUncertain significance GRCh37 chr21: 44,270,159-44,329,131 , GRCh38.p12 chr21: 42,850,049-42,909,021 LOC105372817, NDUFV3, 1 more genes
    nsv7076046inversion1nstd229human GRCh38 chr21: 42,633,367-44,550,173 , GRCh37.p13 chr21: 44,053,477-45,916,560 MYL6P1, MIR5692B, 68 more genes
    nsv7072799inversion1nstd229human GRCh38 chr21: 41,886,117-43,786,596 , GRCh37.p13 chr21: 43,306,226-45,206,477 ZNF295-AS1, LINC01668, 57 more genes
    nsv7064889inversion1nstd229human GRCh38 chr21: 41,632,756-44,900,321 , GRCh37.p13 chr21: 43,052,916-46,320,236 RNU6-1150P, LOC105372824, 123 more genes
    nsv7061709inversion1nstd229human GRCh38 chr21: 42,835,038-42,928,017 , GRCh37.p13 chr21: 44,255,148-44,348,127 WDR4, ERVH48-1, 2 more genes
    nsv7038069copy number variation1nstd229human GRCh38 chr21: 42,886,006-42,890,389 , GRCh37.p13 chr21: 44,306,116-44,310,499 WDR4, LOC105372817
    nsv7037856copy number variation1nstd229human GRCh38 chr21: 42,864,101-42,893,000 , GRCh37.p13 chr21: 44,284,211-44,313,110 LOC105372817, WDR4, 1 more genes
    nsv7036780copy number variation1nstd229human GRCh38 chr21: 42,852,401-42,898,300 , GRCh37.p13 chr21: 44,272,511-44,318,410 WDR4, NDUFV3, 1 more genes
    nsv7036277copy number variation1nstd229human GRCh38 chr21: 42,884,649-42,886,662 , GRCh37.p13 chr21: 44,304,759-44,306,772 WDR4, LOC105372817
    nsv7035695copy number variation1nstd229human GRCh38 chr21: 42,852,339-42,898,334 , GRCh37.p13 chr21: 44,272,449-44,318,444 NDUFV3, WDR4, 1 more genes
    nsv7035339copy number variation1nstd229human GRCh38 chr21: 42,864,564-42,867,944 , GRCh37.p13 chr21: 44,284,674-44,288,054 WDR4
    nsv7032606copy number variation1nstd229human GRCh38 chr21: 42,846,382-42,858,399 , GRCh37.p13 chr21: 44,266,492-44,278,509 WDR4
    nsv7032422copy number variation1nstd229human GRCh38 chr21: 42,859,178-42,861,186 , GRCh37.p13 chr21: 44,279,288-44,281,296 WDR4
    nsv7031971copy number variation1nstd229human GRCh38 chr21: 42,841,069-42,841,098 , GRCh37.p13 chr21: 44,261,179-44,261,208 WDR4
    nsv7031492copy number variation1nstd229human GRCh38 chr21: 42,861,315-42,921,111 , GRCh37.p13 chr21: 44,281,425-44,341,221 NDUFV3, WDR4, 2 more genes
    nsv7031200copy number variation1nstd229human GRCh38 chr21: 42,855,637-42,865,057 , GRCh37.p13 chr21: 44,275,747-44,285,167 WDR4
    nsv7030680copy number variation1nstd229human GRCh38 chr21: 42,890,891-42,898,514 , GRCh37.p13 chr21: 44,311,001-44,318,624 NDUFV3, WDR4
    nsv7027550copy number variation1nstd229human GRCh38 chr21: 42,814,191-42,846,931 , GRCh37.p13 chr21: 44,234,301-44,267,041 WDR4
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